Responsibility Prepare, review, and submit regulatory applications, registrations, renewals, and amendments to regulatoryauthorities. Ensure compliance with SFDA, MOH, and other applicable healthcare regulations and standards. Maintain regulatory licenses, registrations, permits, and approvals. Coordinate with manufacturers, suppliers, and internal departments regarding regulatory requirements. Monitor changes in healthcare regulations and assess their impact on products and operations. Support inspections, audits, and regulatory assessments conducted by authorities. Maintain accurate regulatory documentation and records. Review product labeling, promotional materials, and technical documentation to ensure regulatorycompliance. Follow up on regulatory submissions and respond to inquiries from regulatory authorities. Provide regulatory guidance and awareness to internal stakeholders. Strong knowledge of SFDA and MOH regulations. Understanding of healthcare regulatory processes and product registration requirements. Excellent communication and coordination skills. Strong attention to detail and documentation management. Analytical and problem-solving abilities. Proficiency in Microsoft Office and regulatory systems
Education Bachelor’s degree in pharmacy, Medical Laboratory Sciences, Biotechnology, Life Sciences, or a related healthcare field
Experience2 - 5 years ó „€within the healthcare, pharmaceutical, medical devices, or healthcare services sector.ó „€